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J. Bacteriol., Aug 1995, 4501-4507, Vol 177, No. 15
MA Schembri, RC Bayly and JK Davies
The polyhydroxyalkanoic acid (PHA) biosynthetic gene locus was cloned and
characterized from an Acinetobacter sp. isolated from activated sludge.
Nucleotide sequence analysis identified three clustered genes, phaAAc
(encoding a beta-ketothiolase), phaBAc (encoding an acetoacetyl coenzyme A
reductase), and phaCAc (encoding a PHA synthase). In addition, an open
reading frame (ORF1) with potential to encode a 13- kDa protein was
identified within this locus. The sequence of the putative translational
product of ORF1 does not show significant similarity to any sequences in
the database. A plasmid containing the Acinetobacter pha locus conferred
the ability to accumulate poly-beta- hydroxybutyrate on its Escherichia
coli host. These genes appear to lie in an operon transcribed by two
promoters upstream of phaBAc, an apparent constitutive promoter, and a
second promoter induced by phosphate starvation and under pho regulon
control. These as well as a number of additional potential transcription
start points were identified by a combination of primer extension and
promoter- chloramphenicol acetyltransferase gene fusion studies carried out
in Acinetobacter or E. coli transformants.
Copyright © 1995, American Society for Microbiology
Phosphate concentration regulates transcription of the Acinetobacter polyhydroxyalkanoic acid biosynthetic genes
Department of Microbiology, Monash University, Clayton, Victoria, Australia.
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